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Pediatric Post-operative Abdominal Wound Dehiscence in Association With Midline vs Other Incisions: A Prospective Cohort Study

F

French Medical Institute for Mothers and Children

Status

Completed

Conditions

Wound Dehiscence
Incision

Treatments

Procedure: laparatomy

Study type

Observational

Funder types

Other

Identifiers

NCT05963477
40-FMIC-ER-18

Details and patient eligibility

About

This study is designed to see different abdominal incisions complication among neonates, infants and children and to find risk factors for developing wound dehiscence

Enrollment

270 patients

Sex

All

Ages

1 day to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

-all abdominal surgeries patient under 18-year-old.

Exclusion criteria

  • Umbilical hernia, redo laparatomy, laparoscopic surgery.

Trial design

270 participants in 6 patient groups

Age Group
Description:
Neonates Infants Children
Treatment:
Procedure: laparatomy
Gender
Description:
Male Female
Treatment:
Procedure: laparatomy
Selective/Emergency
Description:
Selective Emergency
Treatment:
Procedure: laparatomy
Wound Class
Description:
Clean Clean-contaminated Contaminated Infected
Treatment:
Procedure: laparatomy
Risk Factors
Description:
Yes No
Treatment:
Procedure: laparatomy
Type of Incisions
Description:
Midline Trransverse Oblique
Treatment:
Procedure: laparatomy

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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